A multi-centre, tolerability study of a cannabidiol-enriched Cannabis Herbal Extract for chronic headaches in adolescents: The CAN-CHA protocol.

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES PLoS ONE Pub Date : 2024-09-20 eCollection Date: 2024-01-01 DOI:10.1371/journal.pone.0290185
Manik Chhabra, Evan C Lewis, Robert Balshaw, Breanne Stewart, Zina Zaslawski, Trinity Lowthian, Zahra Alidina, Melila Chesick-Gordis, Wenli Xie, Britt I Drögemöller, Galen E B Wright, Kathryn A Birnie, Katelynn E Boerner, Vivian W L Tsang, Samantha Lee Irwin, Daniela Pohl, Alexander G Weil, Erick Sell, Erika Penz, Amy Robson-MacKay, Sophia Mbabaali, Stephanie Blackman, Shanlea Gordon, Jane Alcorn, Richard J Huntsman, Tim F Oberlander, G Allen Finley, Lauren E Kelly
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Abstract

Introduction: Cannabis products have been used in the management of headaches in adults and may play a role in pediatric chronic pain. Canadian pediatricians report increasing use of cannabis for the management of chronic headaches, despite no well-controlled studies to inform its dosing, safety, and effectiveness. The aim of our clinical trial is to determine the dosing and safety of a Cannabidiol (CBD)-enriched Cannabis Herbal Extract (CHE) for the treatment of chronic headaches in adolescents.

Methods and analysis: Youth, parents, and an expert steering committee co-designed this tolerability study. Twenty adolescents (aged 14 to 17 years), with a chronic migraine diagnosis for more than 6 months that has not responded to other therapies will be enrolled into an open label, dose escalation study across three Canadian sites. Study participants will receive escalating doses of a CBD-enriched CHE (MPL-001 with a THC:CBD of 1:25), starting at 0.2-0.4 mg/kg of CBD per day and escalating monthly up to 0.8-1.0 mg/kg of CBD per day. The primary objective of this study is to determine the safety and tolerability of CBD-enriched CHE in adolescents with chronic migraine. Secondary objectives of this study will inform the development of subsequent randomized controlled trials and include investigating the relationship between the dose escalation and change in the frequency of headache, impact and intensity of pain, changes in sleep, mood, function, and quality of life. Exploratory outcomes include investigating steady-state trough plasma levels of bioactive cannabinoids and investigating how pharmacogenetic profiles affect cannabinoid metabolism among adolescents receiving CBD-enriched CHE.

Discussion: This protocol was co-designed with youth and describes a tolerability clinical trial of CBD-enriched CHE in adolescents with chronic headaches that have not responded to conventional therapies. This study is the first clinical trial on cannabis products in adolescents with chronic headaches and will inform the development of future comparative effectiveness clinical trials.

Trial registration: CAN-CHA trial is registered with ClinicalTrials.gov with a number of register NCT05337033.

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一项关于富含大麻二酚的大麻草本提取物治疗青少年慢性头痛的多中心耐受性研究:CAN-CHA 方案。
简介:大麻产品已被用于治疗成人头痛,并可能在儿科慢性疼痛中发挥作用。加拿大儿科医生报告称,尽管没有很好控制的研究来说明大麻的剂量、安全性和有效性,但越来越多的人使用大麻来治疗慢性头痛。我们的临床试验旨在确定富含大麻二酚(CBD)的大麻草本提取物(CHE)治疗青少年慢性头痛的剂量和安全性:青少年、家长和专家指导委员会共同设计了这项耐受性研究。20名青少年(14至17岁)被诊断患有慢性偏头痛6个月以上,且对其他疗法无效,他们将在加拿大的三个地点参加一项开放标签、剂量递增研究。研究参与者将逐步接受富含 CBD 的 CHE(MPL-001,四氢大麻酚与 CBD 的比例为 1:25),从每天 0.2-0.4 毫克/千克 CBD 开始,每月递增至每天 0.8-1.0 毫克/千克 CBD。这项研究的主要目的是确定富含CBD的CHE对慢性偏头痛青少年的安全性和耐受性。本研究的次要目标将为后续随机对照试验的开发提供信息,包括调查剂量升级与头痛频率变化、疼痛的影响和强度、睡眠变化、情绪、功能和生活质量之间的关系。探索性结果包括调查生物活性大麻素的稳态谷值血浆水平,以及调查药物遗传特征如何影响接受富含 CBD 的 CHE 的青少年的大麻素代谢:本方案是与青少年共同设计的,描述了对常规疗法无效的慢性头痛青少年进行的富含 CBD 的 CHE 耐受性临床试验。这项研究是首个针对患有慢性头痛的青少年的大麻产品临床试验,将为未来的比较有效性临床试验的发展提供参考:CAN-CHA 试验已在 ClinicalTrials.gov 注册,注册号为 NCT05337033。
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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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